Activation of an IL6 Inflammatory Loop Mediates Trastuzumab Resistance in HER2+Breast Cancer by Expanding the Cancer Stem Cell Population

被引:477
作者
Korkaya, Hasan [1 ]
Kim, Gwang-il [1 ,2 ]
Davis, April [1 ]
Malik, Fayaz [1 ,3 ]
Henry, N. Lynn [1 ]
Ithimakin, Suthinee [1 ]
Quraishi, Ahmed A. [1 ]
Tawakkol, Nader [1 ]
D'Angelo, Rosemarie [1 ]
Paulson, Amanda K. [1 ]
Chung, Susan [1 ]
Luther, Tahra [1 ]
Paholak, Hayley J. [1 ]
Liu, Suling [1 ]
Hassan, Khaled A. [1 ]
Zen, Qin [1 ]
Clouthier, Shawn G. [1 ]
Wicha, Max S. [1 ]
机构
[1] Univ Michigan, Ctr Comprehens Canc, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] CHA Univ, CHA Bundang Med Ctr, Dept Pathol, Songnam 463712, Gyeonggi, South Korea
[3] Indian Inst Integrat Med, Dept Canc Pharmacol, Jammu 180001, India
基金
美国国家卫生研究院;
关键词
HUMAN-BREAST-CANCER; INTERLEUKIN-6; IL-6; TUMOR; SURVIVAL; IDENTIFICATION; TUMORIGENESIS; MECHANISMS; MODEL; PTEN;
D O I
10.1016/j.molcel.2012.06.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although inactivation of the PTEN gene has been implicated in the development of resistance to the HER2 targeting antibody trastuzumab, the mechanisms mediating this resistance remain elusive. We generated trastuzumab resistant cells by knocking down PTEN expression in HER2 overexpressing breast cancer cell lines and demonstrate that development of trastuzumab resistance in these cells is mediated by activation of an IL6 inflammatory feedback loop leading to expansion of the cancer stem cell (CSC) population. Long term trastuzumab treatment generates highly enriched CSCs which display an EMT phenotype secreting over 100-fold more IL6 than parental cells. An IL6 receptor antibody interrupted this inflammatory feedback loop reducing the cancer stem cell population resulting in decreased tumor growth and metastasis in mouse xenographs. These studies demonstrate that trastuzumab resistance may be mediated by an IL6 inflammatory loop and suggest that blocking this loop may provide alternative strategy to overcome trastuzumab resistance.
引用
收藏
页码:570 / 584
页数:15
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